Canonical Allele Identifier: CA1519888758

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205006_186205007delinsAG , CM000666.2:g.186205006_186205007delinsAG	GRCh38
NC_000004.11:g.187126160_187126161delinsAG , CM000666.1:g.187126160_187126161delinsAG	GRCh37
NC_000004.10:g.187363154_187363155delinsAG	NCBI36
NG_007965.1:g.18487_18488delinsAG
NG_012095.2:g.1028_1029delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-194_988-193delinsAG MANE Select	ENSP00000368079.4:n.988-194_988-193delins...
ENST00000378802.4:c.988-194_988-193delinsAG	ENSP00000368079.4:n.988-194_988-193delins...
ENST00000502665.1:n.170_171delinsAG
ENST00000507209.5:n.5492_5493delinsAG
ENST00000513354.5:n.78-194_78-193delinsAG
NM_207352.3:c.988-194_988-193delinsAG	NP_997235.3:n.988-194_988-193delinsAG
XM_005262935.2:c.988-194_988-193delinsAG	XP_005262992.1:n.988-194_988-193delinsAG
XM_006714184.2:c.592-194_592-193delinsAG	XP_006714247.1:n.592-194_592-193delinsAG
XM_005262935.4:c.988-194_988-193delinsAG	XP_005262992.1:n.988-194_988-193delinsAG
XM_017008037.1:c.592-194_592-193delinsAG	XP_016863526.1:n.592-194_592-193delinsAG
NM_207352.4:c.988-194_988-193delinsAG MANE Select	NP_997235.3:n.988-194_988-193delinsAG